Classifications

• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
  • C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
  • C10M133/38—Heterocyclic nitrogen compounds
  • C10M133/44—Five-membered ring containing nitrogen and carbon only
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  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
  • C10M141/06—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic nitrogen-containing compound
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  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
  • C10M141/12—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic compound containing atoms of elements not provided for in groups C10M141/02 - C10M141/10
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  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
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  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
  • C10M169/04—Mixtures of base-materials and additives
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
  • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
  • C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
  • C10M2215/064—Di- and triaryl amines
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
  • C10M2215/22—Heterocyclic nitrogen compounds
  • C10M2215/223—Five-membered rings containing nitrogen and carbon only
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
  • C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
  • C10M2215/30—Heterocyclic compounds
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
  • C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
  • C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
  • C10M2219/066—Thiocarbamic type compounds
  • C10M2219/068—Thiocarbamate metal salts
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
  • C10M2227/06—Organic compounds derived from inorganic acids or metal salts
  • C10M2227/066—Organic compounds derived from inorganic acids or metal salts derived from Mo or W
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
  • C10M2227/09—Complexes with metals
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2010/00—Metal present as such or in compounds
  • C10N2010/12—Groups 6 or 16
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
  • C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
  • C10N2030/10—Inhibition of oxidation, e.g. anti-oxidants
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
  • C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
  • C10N2030/36—Seal compatibility, e.g. with rubber
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2040/00—Specified use or application for which the lubricating composition is intended
  • C10N2040/25—Internal-combustion engines
  • C10N2040/252—Diesel engines
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2070/00—Specific manufacturing methods for lubricant compositions
  • C10N2070/02—Concentrating of additives

Definitions

• the invention describes a new composition that is effective at reducing the Cu and Pb corrosion of engine oils containing high levels of organo-molybdenum compounds.
• the invention also describes new engine oil compositions containing high levels of molybdenum that are resistant to Cu and Pb corrosion.
• the invention also describes a method of reducing Cu and Pb corrosion in engine oils formulated with high levels of organomolybdenum compounds.
• the composition comprises (A) a sulfur-containing organo-molybdenum compound, (B) a sulfur-free organo-molybdenum compound, and (C) triazole or a derivatized triazole.
• the new engine oil compositions comprise: (A) a sulfur-containing organo- molybdenum compound, (B) a sulfur-free organo-molybdenum compound, (C) triazole or a derivatized triazole, (D) one or more base oils, and, optionally, (E) one or more additives selected from the group including antioxidants, dispersants, detergents, anti- wear additives, extreme pressure additives, friction modifiers, rust inhibitors, corrosion inhibitors, seal swell agents, anti-foaming agents, pour point depressants and viscosity index modifiers.,
• the method of reducing Cu and Pb corrosion involves adding the above composition, either as a blend, as individual components or as a blend or individual components in combination with the optional additives described in (E), to a lubricating engine oil that is determined to be corrosive to Cu and/ or Pb as determined by the High Temperature Corrosion Bench Test ASTM D 6594 when at least one of A, B or C are not present.
• An oil corrosive to Cu is one that reports an end of test used oil Cu level increase above the 20 ppm maximum for the heavy duty diesel CJ-4 specification.
• An oil corrosive to Pb is one that reports an end of test used oil Pb level increase above the 120 ppm maximum for the heavy duty diesel CJ-4 specification.
• U. S. Application 20100173808 and 20080200357 describe the use of derivatized triazoles, but molybdenum is not present or mentioned.
• U. S. Application 20040038835 describes derivatized triazoles but does not teach the use of combinations of molybdenum compounds.
• U. S. Patent 5580482 describes derivatized triazoles used in triglyceride ester oils but molybdenum is not mentioned or present.
• organo-molybdenum compounds in lubricants provides a number of beneficial properties including oxidation protection, wear protection and friction reduction for improved fuel economy performance.
• molybdenum compounds that are utilized to achieve these benefits. They are the sulfur-containing organo-molybedum compounds, of which the molybdenum dithiocarbamates and tri-nuclear organo-molybdenum compounds are the best known, and the sulfur-free organo-molybdenum compounds of which the organo-molybdate esters and molybdenum carboxylates are the best known.
• These products provide valuable benefits to lubricants but also have limitations.
• This invention allows the use of significantly higher levels of organo-molybdenum compounds (at least up to 320 ppm, and possibly up to 800 ppm) in engine oil formulations that are required to pass the High Temperature Corrosion Bench Test ASTM D 6594.
• corrosivity of engine oil formulations were also evaluated by modifying the temperature and test duration used in ASTM D 6594 where a higher temperature and shorter test duration compared to ASTM D 6594 were used.
• These include primarily heavy duty diesel engine oils.
• the invention should have utility in any engine oil formulation where Cu and Pb corrosion can be a problem.
• passenger car engine oils examples include passenger car engine oils, marine diesel oils, railroad diesel oils, natural gas engine oils, racing oils, hybrid engine oils, turbo-charged gasoline and diesel engine oils, engine oils used in engines equipped with direct injection technology, and two- and four-cycle internal combustion engines.
• U. S. Application 20040038835 describes derivatized triazoles and teaches their use with either sulfur-containing or sulfur-free organo-molybdenum compounds, but does not teach the combination of both sulfur-free and sulfur-containing organo-molybdenum compounds as being critical to achieving both Cu and Pb corrosion protection, and further does not teach the use of these compounds to reduce copper corrosion. Only reduction of Pb corrosion is taught.
• This invention will provide the ability to use higher levels of organomolybdenum in heavy duty diesel engine oils to solve a variety of possible performance problems including improved oxidation control, improved deposit control, better wear
• This invention may represent a very cost effective way to provide a small increase in molybdenum content of heavy duty diesel engine oils.
• Most heavy duty diesel oils today do not contain molybdenum, or if they do at very low levels (less than 50 ppm).
• This invention could allow the use of 50 to 800 ppm, preferably 75-320 ppm of molybdenum in a very cost effective way. Higher levels of molybdenum are possible with this technology but at a higher cost.
• Component A Sulfur-containing organo-molybdenum compounds
• the sulfur-containing organo-molybdenum compound may be mono-, di-, tri- or tetra- nuclear as described in U. S. Patent 6723685. Dinuclear and trinuclear sulfur-containing organo-molybdenum compounds are preferred. More preferably, the sulfur-containing organo-molybdenum compound is selected from the group consisting of molybdenum dithiocarbamates (MoDTC), molybdenum dithiophosphates (MoDTP), molybdenum dithiophosphinates, molybdenum xanthates, molybdenum thioxanthates, molybdenum sulfides and mixtures thereof.
• MoDTC molybdenum dithiocarbamates
• MoDTP molybdenum dithiophosphates
• molybdenum dithiophosphinates molybdenum xanthates
• molybdenum thioxanthates mo
• the sulfur-containing organo-molybdenum compounds that may be used include tri- nuclear molybdenum-sulfur compounds as described in European Patent Specification EP 1 040 115 and U. S. Patent 6232276, molybdenum dithiocarbamates as described in U. S. Patents 4098705, 4178258, 5627146, and U. S. Patent Application 20120264666, sulfurized oxymolybdenum dithiocarbamates as described in U. S. Patent 3509051 and 6245725, molybdenum oxysulfide dithiocarbamates as described in U. S. Patent 3356702 and 5631213, highly sulfurized molybdenum dithiocarbamates as described in U. S.
• Patent 7312348 highly sulfurized molybdenum oxysulfide dithiocarbamates as described in U. S. Patent 7524799, imine molybdenum dithiocarbamate complexes as described in U. S. Patent 7229951, molybdenum dialkyl dithiophosphates as described in Japanese Patents 62039696 and 10121086 and U. S. Patents 3840463, 3925213 and 5763370, sulfurized oxymolybdenum dithiophosphates as described in Japanese Patent 2001040383, oxysulfurized molybdenum dithiophosphates as described in Japanese Patents 2001262172 and 2001262173, and molybdenum phosphorodithioates as described in U. S. Patent 3446735.
• sulfur containing organo-molybdenum compounds may be part of a lubricating oil dispersant as described in U. S. Patents 4239633, 4259194, 4265773 and 4272387, or part of a lubricating oil detergent as described in U. S. Patent 4832857.
• Examples of commercial sulfur-containing organo-molybdenum compounds that may be used include MOLYVAN 807, MOLYVAN 822 and MOLYVAN 2000, and
• MOLYVAN 3000 which are manufactured by Vanderbilt Chemicals, LLC, and
• SAKURA-LUBE 165 and SAKURA-LUBE 515 which are manufactured by Adeka Corporation, and Infineum C9455, which is manufactured by Infineum International Ltd.
• the treat level of the sulfur-containing organo-molybdenum compound in the engine oil compositions may be any level that will result in Cu and/ or Pb corrosion as determined by the High Temperature Corrosion Bench Test ASTM D 6594. Actual treat levels can vary from 25 to 1000 ppm molybdenum metal and will vary based on the amount of components B and C, the engine oil additives present in the formulation and the base oil type used in the finished lubricant.
• Preferred levels of sulfur-containing organo-molybdenum are 50 to 500 ppm molybdenum metal and the most preferred levels are 75 to 350 ppm molybdenum metal.
• Component B Sulfur-free organo-molybdenum compounds
• the sulfur-free organo-molybdeum compounds that may be used include organo- amine complexes with molybdenum as described in U. S. Patent 4692256, glycol molybdate complexes as described in U. S. Patent 3285942, molybdenum imide as described in U. S. Patent Application 20120077719, organo-amine and organo-polyol complexes with molybdenum as described in U. S. Patent 5143633, sulfur-free organo- molybdenum compounds with high molybdenum content as described in U. S.
• Patents 6509303, 6645921 and 6914037 molybdenum complexes prepared by reacting a fatty oil, diethanolamine and a molybdenum source as described in U. S. Patent 4889647; an organomolybdenum complex prepared from fatty acids and 2-(2-aminoethyl) aminoethanol as described in U. S. Patent 5137647, 2,4-heteroatom substituted- molybdena-3,3-dioxacycloalkanes as described in U. S. Patent 5412130, and
• sulfur-free organo-molybdenum compounds may be part of a lubricating oil dispersant as described in U. S. Patents 4176073, 4176074, 4239633, 4261843, and 4324672, or part of a lubricating oil detergent as described in U. S. Patent 4832857.
• Examples of commercial sulfur-free organo-molybdenum compounds that may be used include MOLYVAN 855, which is manufactured by Vanderbilt Chemicals, LLC, SAKURA-LUBE 700 which is manufactured by Adeka Corporation, and 15%
• Molybdenum HEX-CEM which is manufactured by OM Group Americas, Inc.
• the treat level of the sulfur-free organo-molybdenum compound in the engine oil compositions may be any level that will result in Cu and/ or Pb corrosion as determined by the High Temperature Corrosion Bench Test ASTM D 6594. Actual treat levels can vary from 25 to 1000 ppm molybdenum metal and will vary based on the amount of components A and C, the engine oil additives present in the formulation and the base oil type used in the finished lubricant.
• Preferred levels of sulfur-free organo- molybdenum are 50 to 500 ppm molybdenum metal and the most preferred levels are 75 to 350 ppm molybdenum metal.
• triazoles and derivatized triazoles are not tolutriazoles or benzotriazoles, or derivatized tolutriazoles or benzotriazoles. This is an important distinction in their ability to function as effective corrosion inhibitors when in the presence of sulfur-free organo-molybdenum compounds and sulfur-containing organo- molybdenum compounds. It is believed that the derivatized triazoles of this invention are made more effective due to the absence of a fused aromatic ring.
• 1,2,4-Triazole may be used in this invention but is not preferred due to its volatility and poor solubility in lubricants. However, it is contemplated that 1,2,4-triazole, if solubilized and under certain application conditions, can be effective.
• the derivatized triazoles are prepared from 1,2,4-triazole (triazole), a formaldehyde source and alkylated diphenylamine by means of the Mannich reaction. These reactions are described in U.S. Patent 4,734,209 where the alkylated diphenylamine is replaced by various secondary amines, and in U. S. Patent 6,184,262, where the triazole is replaced by benzotriazole or tolutriazole. Water is a by-product of the reaction.
• the reaction may be carried out in a volatile organic solvent, in a diluent oil or in the absence of a diluent.
• a volatile organic solvent in general the solvent is removed by distillation after the reaction is complete.
• a slight stoichiometric excess of either the 1,2,4-triazole, the formaldehyde source, or the alkylated diphenylamine may be used without adversely affecting the utility of the final product isolated.
• the derivatized triazole may have one of three possible structures where Rl and R2 represent hydrogen, or the same or different linear or branched hydrocarbyl groups from 1 to 30 carbons, or hydrogen, or the same or different alkaryl groups from 7 to 30 carbons, or hydrogen, or the same or different aryl groups from 6 to 10 carbons, and R3 represents hydrogen, or a linear or branched alkyl group from 1 to 30 carbons.
• R3 is hydrogen
• Rl and R2 are alkyl or alkylphenyl: lH-l,2,4-triazole-l-methanamine, N,N-bis(alkyl)- N,N-bis(alkyl)-((l,2,4-triazol-l-yl)methyl)amine
• triazoles examples include: l-iN / N-bisimethy ⁇ aminomethy ⁇ -l ⁇ -triazole
• the derivatized triazole may be a bis-triazole as shown below:
• X may be a linear or branched hydrocarbyl group from 1 to 30 carbons, or a polyalkylene glycol group -(C ⁇ ClH O ClH ClH -, where y can vary from 1 to 250.
• the derivatized triazole may be part of a lubricating oil dispersant as described in U. S. Patents 4908145, 5049293, 5080815 and 5362411.
• Preferred derivatized triazoles are the alkylated diphenylamine derivatives of triazoles described in U. S provisional application serial number 62/205250 filed August 14, 2016 by the present applicant.
• alkylated diphenylamine derivatives of triazole being octylated or higher alkylated diphenylamine derivatives of triazole (e.g. nonylated, decylated, undecylated, dodecylated, tridecylated, tetradecylated, pentadecylated, hexadecylated).
• the alkyl groups may be linear, branched or cyclic in nature.
• the novel molecule is l-[di-(4-octylphenyl)aminomethyl]triazole or l-[di-(4- nonylphenyl)aminomethyl] triazole.
• a molecule which has at least one phenyl group being octylated or higher alkyl, where the other phenyl group may be alkylated with C7 or lower, such as C4 would also be effective.
• butyl/ octylphenyl)aminomethyl] triazole which comprises a mixture of l-[ (4- butylphenyl) (phenyl) aminomethyl] triazole, l-[ (4-octylphenyl) (phenyl)
• the effective amount of the mixture of molecules would be based on the proportion of the octylated or higher alkyl which is present.
• the treat level of the derivatized triazole in the engine oil compositions may be any level necessary to reduce Cu and Pb corrosion, or any level necessary to pass the High Temperature Corrosion Bench Test ASTM D 6594 for Cu and Pb when components A and B by themselves fail.
• a practical range is from 0.01 wt% to 0.25 wt% .
• higher level of derivatized triazole may be necessary.
• levels of derivatized triazole well below 0.01 wt % e.g. 0.001 wt%) may be effective.
• Mineral and synthetic base oils may be used including any of the base oils that meet the API category for Group I, 11, 111, IV and V.
• Additional additives are selected from the group including antioxidants, dispersants, detergents, anti-wear additives, extreme-pressure additives, friction modifiers, rust inhibitors, corrosion inhibitors, seal swell agents, anti-foaming agents, pour point depressants and viscosity index modifiers.
• antioxidants dispersants, detergents, anti-wear additives, extreme-pressure additives, friction modifiers, rust inhibitors, corrosion inhibitors, seal swell agents, anti-foaming agents, pour point depressants and viscosity index modifiers.
• anti-wear additives contain phosphorus.
• the additional additives would include one or more dispersants, one or more calcium or magnesium overbased detergents, one or more antioxidants, zinc dialkyldithiophosphate as the anti-wear additive, one or more organic friction modifiers, a pour point depressant and one or more viscosity index modifiers.
• Optional additional additives used in heavy duty diesel engine oils include: (1) supplemental sulfur-based, phosphorus-based or sulfur- and phosphorus-based anti-wear additives. These supplemental anti-wear additives may contain ash producing metals (Zinc, Calcium, Magnesium, Tungsten, and Titanium for example) or they may be ashless, (2) supplemental antioxidants including sulfurized olefins, and sulfurized fats and oils.
• ash producing metals Zinc, Calcium, Magnesium, Tungsten, and Titanium for example
• the method of reducing Cu and Pb corrosion involves adding to an engine oil that fails the High Temperature Corrosion Bench Test ASTM D 6594 for Cu and/ or Pb corrosion one or more of A, B and C depending on what is already present in the formulation. For example, if an engine oil fails ASTM D 6594 and contains A and B, the method would involve adding C. If an engine oil fails ASTM D 6594 and contains A and C, the method would involve adding B. If an engine oil fails ASTM D 6594 and contains B and C, the method would involve adding A. If an engine oil fails ASTM D 6594 and contains only A, the method would involve adding B and C. If an engine oil fails ASTM D 6594 and contains only B, the method would involve adding A and C. If an engine oil fails ASTM D 6594 and contains only C, the method would involve adding A and B. The method may also involve adding a blend of A, B and C to an engine oil that fails the ASTM D 6594 when one of A, B or C are not present.
• the additive combinations of this invention are effective top treats to existing heavy duty diesel engine oil formulations.
• a blend of Components A, B and C would permit the use of high levels of molybdenum for achieving higher performance attributes while still controlling Cu and Pb corrosion.
• a method of enhancing the performance of a heavy duty diesel engine oil would involve adding to the heavy duty diesel engine oil a blend of Component A, B and C.
• the invention contemplates an engine oil, particularly a heavy duty diesel engine oil, having components A, B and C present, each component being present either as part of the engine oil formulation, or as an additive.
• the lubricating composition of the invention comprises a major amount of base oil (e.g. at least 80%, preferably at least 85% by weight) and an additive composition comprising:
• (C) triazole or a derivatized triazole may be present in the lubricating composition in an amount which together provides about 50-800 ppm molybdenum, preferably about 75-320 ppm molybdenum.
• a ratio of (A):(B) based on the amount of molybdenum provided by each may be from about 0.25:1 to 4:1, preferably about 0.5:1 to 2:1, and most preferably at about 1:1.
• (C) is present in the lubricating composition in an amount between 0.001 wt. % and 1.0 wt. %, preferably between 0.005 and 0.4 wt.% .
• the amount of derivatized triazole may be correlated to the total amount of molybdenum, such that at lower molybdenum amounts, less triazole is needed.
• (A) and (B) together provide between about 50-200 ppm molybdenum, preferably about 120 ppm Mo
• (C) is present at between about 0.005-0.05 wt % .
• (A) and (B) together provide between about 250-500 ppm molybdenum, preferably about 320 ppm Mo
• (C) is present at between about 0.1-0.5 wt%, preferably about 0.2-0.4 wt%.
• the invention also contemplates an additive concentrate for adding to a lubricating composition, the additive concentrate comprising components (A), (B) and (C) as above, wherein the ratio of (A):(B) based on the amount of molybdenum provided by each may be from about 0.25:1 to 4:1, preferably about 0.5:1 to 2:1, and most preferably at about 1:1; and the weight ratio of [the total of (A) + (B)]:(C) is from about 50:1 to 1:2, preferably about 33:1 to 1:1.
• An exemplary product may contain a blend of MOLYVAN® 855 (sulfur-free) molybdenum ester/ amide complex from Vanderbilt Chemicals, LLC, and one or more of sulfur-containing molybdenum additives such as MOLYVAN® 3000 or 822 molybdenum dithiocarbamates, MOLYVAN® L Molybdenum di (2-ethylhexyl) phosphorodithioate, all from from Vanderbilt Chemicals, LLC , or Sakuralube® 525 molybdenum dithiocarbamate from Adeka Corporation.; in the presence of
• IRGAMET® 30 (derivatized triazole l-(di-(2-ethylhexyl)aminomethyl)-l,2,4-triazole) from BASF Corp.
• Blend A at 1.0 wt. % in a finished engine oil would deliver 360 ppm Mo from MOLYVAN 855, 360 ppm Mo from MOLYVAN 3000, and 0.19 wt. % IRGAMET 30.
• Blend B at 0.25 wt. % in a finished engine oil would deliver 100 ppm Mo from
• MOLYVAN 855 100 ppm Mo from MOLYVAN 3000, and 0.025 wt. % IRGAMET 30. It is expected that with reduced levels of Mo in the engine oil, e.g. down to 100 ppm or less, IRGAMET 30 may be effective in reducing corrosion at extremely low levels, e.g. down to 0.01 wt% or lower.
• HTCBT high temperature corrosion bench test
• ASTM D 6594 test method Details of the test method can be found in the annual book of ASTM standards.
• the test lubricant was kept at 135°C and dry air was bubbled through the lubricant at 5 ⁇ 0.5 L/h for 1 week.
• API CJ - 4 specifications for heavy duty diesel engine oil limits the metal concentration of copper and lead in the oxidized oil as per ASTM D 6594 test methods to 20 ppm maximum and 120 ppm maximum respectively.
• ICP inductive coupled plasma
• base blend is SAE 15W-40 viscosity grade fully formulated heavy duty diesel engine oil consisting of one or more base oils, dispersants, detergents, VI
• Molybdenum dithiocarbamate (A) is a commercial branched tridecyl amine based molybdenum dithiocarbamate containing 10 % molybdenum by weight available from Vanderbilt Chemicals, LLC as MOLYVAN® 3000.
• Molybdenum Ester/ Amide is a commercial molybdate ester containing 8 % molybdenum by weight available from Vanderbilt Chemicals, LLC as MOLYVAN® 855.
• 1,2,4-Triazole (C) is l-(N,N-bis(2-ethylhexyl)aminomethyl)-l,2,4- triazole. All the formulations in Table 1 have a total molybdenum content of 150 ppm. In examples 1A thru IB, when only a single molybdenum source is used (either sulfur- containing molybdenum (A) or sulfur-free molybdenum (B)) and triazole C is not present, the passing rate in the HTCBT is very low (16.6% for Cu and 66.66% for Pb).
• Base Blend is fully formulated heavy duty diesel engine oil with SAE 15W40 viscosity grade Table IB Components (wt. %)
• base blend is SAE OW-20 viscosity grade fully formulated engine oil consisting of one or more base oils, dispersants, detergents, VI Improvers, antioxidants, antiwear agents, pour point depressants and any other additives such that when combined with the invention makes a fully formulated motor oil. Base blend is then further formulated as described in the examples shown in table 2-6.
• HTCBT high temperature corrosion bench test
• ICP inductive coupled plasma
• Molybdenum dithiocarbamate (D) is a commercial mixed tridecyl/2-ethylhexyl amine based molybdenum dithiocarbamate containing 10 % molybdenum by weight available from Adeka Corporation.
• 1,2,4- Triazole (E) is l-(N,N-bis(2-ethylhexyl)aminomethyl)-l,2,4-triazole from a different source compared to (C).
• Molybdenum dithiophosphate (F) is commercial molybdenum di(2-ethylhexyl)phosphorodithioate containing 8.5 % molybdenum by weight available from Vanderbilt Chemicals, LLC.
• Molybdenum Trinuclear (G) is a trinuclear
• molybdenum dithiocarbamate containing 5.5 % molybdenum by weight.
• Molybdenum dithiocarbamate (H) is a tridecyl amine based molybdenum dithiocarbamate containing 6.9 % molybdenum by weight.
• N,N-Bis(2-ethylhexyl)-ar-methyl-lH-benzotriazole-l- methanamine (I) is an alkylamine derivative of tolutriazole corrosion inhibitor available from Vanderbilt Chemicals, LLC as CUV AN® 303.
• 2,5-dimercapto-l,3,4-thiadiazole derivative (J) is a sulfur-based corrosion inhibitor available from Vanderbilt Chemicals LLC as CUV AN® 826.
• the molybdenum content formulated into the lubricants is such that 160 ppm molybdenum is derived from the sulfur-free organo- molybdenum source (B) and approximately 160 ppm molybdenum is derived from a sulfur-containing molybdenum source.
• organomolybdenum (B), sulfur-containing organo-molybdneum (A, D, F, G, H) and 1,2,4-Triazole (C, E) are highly effective at reducing Cu and Pb corrosion in the HTCBT or modified HTCBT. Also, other corrosion inhibitors such as (I) and (J) are ineffective at simultaneously reducing both Cu and Pb corrosion in the HTCBT and modified
• base blend is SAE 15W-40 viscosity grade fully formulated heavy duty diesel engine oil consisting of one or more base oils, dispersants, detergents, VI Improvers, antioxidants, antiwear agents, pour point depressants and any other additives such that when combined with the invention makes a fully formulated motor oil.
• Base blend is then further formulated as described in the examples 30-33. Corrosivity of these formulations towards copper and lead metals was evaluated using high temperature corrosion bench test (HTCBT) according to the ASTM D 6594 test methods. Details of the test method can be found in the annual book of ASTM
• test specimen 100 ⁇ 2 grams of lubricant was used.
• test lubricant was kept at 135°C and dry air was bubbled through at 5 ⁇ 0.5 L/h for 1 week.
• API CJ - 4 specifications for heavy duty diesel engine oil limits the metal concentration of copper and lead in the oxidized oil as per ASTM D 6594 test methods to 20 ppm maximum and 120 ppm maximum respectively.
• lubricant were analyzed for the Cu and Pb metal in the oil using inductive coupled plasma (ICP) analytical technique.
• ICP inductive coupled plasma
• A, B and C are as described previously.
• Dioctylated diphenylamine derivative of 1,2,4- triazole (P-l) was that prepared in Example P-l.
• Butylated/ octylated diphenylamine derivative of 1,2,4-triazole (P-2) was that prepared in example P-2.
• 1,2,4-triazole (C), dioctylated diphenylamine derivative of 1,2,4-triazole (50% active) (P-l), and butylated/ octylated diphenylamine derivative of 1,2,4-triazole (P-2) are all effective to reduce corrosion in the three-way additive system containing sulfur-free organo-molybdenum, sulfur-containing organo- molybdenum and dertivatized triazole.
• Example P-l Preparation of l-(N,N-bis(4-(l,l/3,3- tetramethylbutyl)phenyl)aminomethyl)-l,2,4-triazole in 50% process oil
• VANLUBE® 81 dioctyl diphenylamine
• 1,2,4-triazole 1,2,4-triazole
• Example P-2 Preparation of mixed butylated/ octylated diphenylamine derivative of 1,2,4-triazole in 50% process oil

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